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Identify clearly the procedure to be followed by all parties involved during the different stages
of internal audit implementation and maintenance.
Give detailed explanation of how to complete the activities within the process to be used as a
guideline for ESOM Management and staff.
2.0 Scope
This procedure is applicable to ESOM management and staff.
3.0 Contractual Obligation
This procedure addresses requirements as contained in standards and client contractual documents.
4.0 Controlled Distribution List
Copy No.
Document Owner
Location
Master
IMS Manager
IMS Directory
Document Description
IMS Manual
Requirement
ISO 14001
4.5.4
OSHAS 18001
4.5.4
ISO 9001
8.2.2
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Internal Audit
7.0 Authority and Responsibility
8.2 Output
Audit report.
Corrective and Preventive action reports.
Audit questionnaire
Certification
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Internal Audit
9.0 Process Flow Chart
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Internal Audit
Responsible for planning the Audits and informing HODs Managers of intended audit times
and dates well in advance.
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Internal Audit
Shall retain records of all audits done and raise the relevant corrective and preventive action
reports as required.
IMS Auditor
HOD
Auditees
Types of audits
There are basically four types of audits:
Scheduled Audits,
Un-scheduled Audits,
Client related Audits,
External Audits.
Scheduled
These are formally documented audits on specific areas within ESOM and shall basically cover
compliance with the IMS system and the function and integration of the area (e.g. to identify new
tasks or changes, which require changes to, or new procedures etc.).
Un-scheduled
These audits are done as and when required. They normally occur when an area of non-conformance
(including problems) is identified in a particular area.
Client Audits
These are audits can be done on any projects/sites by any one of our clients if requested. Audits shall
confirm compliance with relevant IMS processes as issued from the IMS Toolbox throughout the
complete life-cycle of a project. If at the time of a project audit the complete life-cycle cannot be
audited than one aspect of the project (i.e. contract review) may be verified.
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Internal Audit
External Audits
These audits shall be completed by a certification body and shall verify compliance to ISO 9001, ISO
14001 and or OHSAS 18001 whichever is applicable. It shall include both the system as well as the
process.
Planning the Audit
The IMS Manager shall be responsible for planning the audit to be done. The audit may either be
scheduled (i.e. from the IMS audit plan) or an un-scheduled audit arranged due to concerns in a
particular area.
The IMS Manager shall be responsible for producing an IMS Audit Plan, which shall highlight the
audits to be done throughout the year within ESOM. The frequency of the audits shall depend on the
areas of risks identified within the client/department/process and their importance and the added
value to ESOM.
The auditor shall prepare for the audit taking into account the following criteria:
From the above information the auditor shall be able to produce an audit checklist / guideline to
serve as an aide memoir for the areas to be audited. The auditor needs to familiarise himself with the
process to be audited and hence make sure detailed questions are prepared for any risk areas.
Inform HOD
The IMS Manager will advise the departments when the applicable Audit will take place at least 24
hours prior to the Audit taking place.
The auditor shall inform the HOD about the intention to do an audit on a particular process.
If the Auditees/process owner cannot make the appointed date and time (i.e. due to other deadlines)
then an alternative date will need to be agreed upon and the audit schedule shall be revised to
accommodate new dates.
Conducting the Audit
Audits shall be carried out by internal auditors on all of ESOM against a defined audit plan twice a
year.
Audits of the IMS, process and/or product shall be carried out by the designated Internal Auditor,
independent of those having direct responsibility for the work being performed. Audits shall be
scheduled for a six month period. All Auditors shall be independent from the activity that they Audit.
Where problem areas are identified, changes will be hand written in by the auditor on the actual
document Audited with a different colour ink than black, signed and dated at the top of each page.
A summary of the results of these audits will be submitted at the Management Review Meetings, and
problem areas identified may be highlighted at these meetings.
The Internal Auditor, or Audit Team, will be nominated by the IMS Manager, prior to the audit.
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Internal Audit
The criteria for internal quality audits are:
a) Does the procedure reflect actual practices?
b) Does the procedure need elaboration to reflect actual practice or must actual practices be changed
back to coincide with procedural requirements.
The auditor cannot check each and every record; hence a sample of records shall be audited. The
auditor shall remember the show me principle and make sure it is used when the Auditees answers,
This is how we do it (i.e. look for evidence whilst the activity is being demonstrated).
A copy of the actual Procedure or document will be used as an Audit checklist, and this document will
be used as the criteria to audit the activity or function. The auditor will date and sign every page of the
document audited, and add comments if applicable.
The actual copy of the Procedure or Work Instruction will be used as a checklist, once the audit is
completed an Audit Report IMS-QAL-04-00000-22 will be generated and suitable corrective action
taken if required.
Unplanned audits will be conducted by a designated Internal Auditor as and when problems or nonconformances arise in any area or process at any time during the year.
The actual Audit Copy of the Policy, Procedure or document will be attached to the Audit Report IMSQAL-04-00000-22 and filed as record of the audit.
Any outstanding actions from previous audits shall be checked and verified as complete before
proceeding with the audit, any CARs outstanding shall be addressed prior to audit start.
Standard Audit Questionnaire
A Standard Audit Questionnaire Working Copy IMS-QAL-04-000-20 is available and can be used to
measure the total implementation of a suitable and effective IMS and the Audit Report and Gap
Analysis Template IMS-QAL-04-000-21 can be completed after completion of this exercise.
Classification of Audit Findings
Critical
Major
Minor
Minor drop-off in the process, which can usually be rectified at the time of the audit.
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Internal Audit
100%
1 week
12.0Audit Points
The following audit points should be checked:
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13.0 Records
The following records are to be held as an outcome of this procedure:
Record No.
Record Description
IMS-QAL-04-00000-20
IMS-QAL-04-00000-22
Audit Report
IMS-QAL-04-00000-23
IMS-QAL-04-00000-24
IMS-QAL-04-00000-27
14.0 Approval
Date
Designation
Name
Signature
IMS Manager
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